Novel indium-mediated ternary reactions between indole-3-carboxaldehydes-allyl bromide-enamines : Facile synthesis of bisindolyl- and indolyl-heterocyclic alkanes

doi:10.1016/S0040-4039(03)00168-0

Paper

Novel indium-mediated ternary reactions between indole-3-carboxaldehydes-allyl bromide-enamines : Facile synthesis of bisindolyl- and indolyl-heterocyclic alkanes

Published Mar 3, 2003 · Subodh Kumar, Vijay Kumar, S. Chimni

Tetrahedron Letters

Q3 SJR score

29

Citations

0

Influential Citations

Full textSemantic Scholar

Abstract

Abstract hidden due to publisher request; this does not indicate any issues with the research. Click the full text link above to read the abstract and view the original source.

Study Snapshot

Indole-3-carboxaldehydes undergo indium-mediated ternary reactions with allyl bromide and indoles to produce bisindolyl and indolyl-heterocyclic alkanes in excellent yields.

PopulationOlder adults (50-71 years)

Sample size24

MethodsObservational

OutcomesBody Mass Index projections

ResultsSocial networks mitigate obesity in older groups.

Novel indium-mediated ternary reactions between indole-3-carboxaldehydes-allyl bromide-enamines : Facile synthesis of bisindolyl- and indolyl-heterocyclic alkanes

References

Citations